EP0726898B1 - Composes de phenylindole - Google Patents

Composes de phenylindole Download PDF

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Publication number
EP0726898B1
EP0726898B1 EP94931520A EP94931520A EP0726898B1 EP 0726898 B1 EP0726898 B1 EP 0726898B1 EP 94931520 A EP94931520 A EP 94931520A EP 94931520 A EP94931520 A EP 94931520A EP 0726898 B1 EP0726898 B1 EP 0726898B1
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Prior art keywords
ethyl
chloro
fluorophenyl
indol
piperidin
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German (de)
English (en)
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EP0726898A1 (fr
Inventor
Jens Kristian Perregaard
Ejner Knud Moltzen
Kim Andersen
Henrik Pedersen
Klaus Peter B Ges
Andre Pernet
Barbara Bopp
Darcy Mulford
Kiyoshi Sakamoto
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H Lundbeck AS
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H Lundbeck AS
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/26—Psychostimulants, e.g. nicotine, cocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives

Definitions

  • the present invention is concerned with a class of novel phenylindole compounds related to the atypical neuroleptic sertindole (1-[2-[4-[5-chloro-1-(4-fluorophenyl)-1 H -indol-3-yl]piperidin-1-yl]ethyl]-2-imidazolidinone), however being substituted in the 4- and/or 5-position of the imidazolidinone ring.
  • Said compounds or a salt or pro-drug thereof are useful as antipsychotics, antidepressants, antihypertensives and/or in the treatment of extrapyramidal side effects induced by antipsychotic drugs and negative symptoms of schizophrenia.
  • US patent No 4,710,500 corresponding to EP 200,322 B discloses in general optionally 5-substituted 1-aryl-3-(4-piperidyl)-, 1-aryl-3-(1-piperazinyl)- or 1-aryl-3-(1,2,3,6-tetrahydro-4-pyridyl)indole derivatives having hydrogen or alkyl, alkenyl or certain heterocycle-lower alkyl substituents at the nitrogen atom in the piperidyl, piperazinyl or tetrahydropyridyl group.
  • the object of the invention is to provide novel drugs having a similar pharmacological profile to that of sertindole, in which drugs, however, the formation of said metabolite is either delayed or prevented.
  • sertindole said major circulating metabolite of sertindole is the compound 1-[2-[4-[5-chloro-1-(4-fluorophenyl)-1 H -indo-3-yl]piperidin-1-yl]ethyl]-1,3-dihydroimidazol-2-one which is structurally identical to sertindole except for the double bond in the 1,3-dihydroimidazol-2-one ring.
  • the present invention relates to novel compounds having general Formula I wherein R 1 - R 4 are independently selected from the group consisting of hydrogen, deuterium, C 1-4 alkyl, and C 1-4 lower alkoxy, with the proviso that all four substituents cannot be hydrogen; or at least one pair of substituents (R 1 ,R 2 or R 3 ,R 4 ) constitutes an oxo group and, if only one oxo group is present, the other two substituents are selected from the above group defined for R 1 - R 4 , with the proviso that they may not both be hydrogen; or R 1 and R 2 and/or R 3 and R 4 , respectively, are joined together to form a 3-8 membered spiro ring; or an acid addition salt thereof.
  • R 1 - R 4 are independently selected from the group consisting of hydrogen, deuterium, C 1-4 alkyl, and C 1-4 lower alkoxy, with the proviso that all four substituents cannot be hydrogen; or at least one pair of substituent
  • the invention relates to a method for the preparation of the novel compounds of Formula I .
  • the invention relates to a pharmaceutical composition
  • a pharmaceutical composition comprising a novel compound of Formula I together with a suitable pharmaceutically acceptable carrier or diluent.
  • the invention relates to the use of the compounds of Formula I for preparing a pharmaceutical composition for treatment of psychosis, depression, negative symptoms of schizophrenia, hypertension or extrapyramidal side effects induced by antipsychotic drugs.
  • the compounds of the invention have been found to show a pharmacological profile similar to that of sertindole, whereas they are not liable to or less liable to transformation of the imidazolidinone ring into a 1,3-dihydroimidazol-2-one ring, which transformation takes place with respect to sertindole.
  • the pharmacological profile of the compounds of the invention indicates that they are useful in the treatment of the above mentioned disorders.
  • the pharmaceutically acceptable acid addition salts of the compounds used in the invention are salts formed with non-toxic organic or inorganic acids.
  • organic salts are those with maleic, fumaric, benzoic, ascorbic, embonic, succinic, oxalic, bis-methylenesalicylic, methanesulfonic, ethanedisulfonic, acetic, propionic, tartaric, salicylic, citric, gluconic, lactic, malic, mandetic, cinnamic, citraconic, aspartic, stearic, palmitic, itaconic, glycolic, p-amino-benzoic, glutamic, benzene sulfonic and theophylline acetic acids, as well as the 8-halotheophyllines, for example 8-bromo-theophylline.
  • inorganic salts are those with hydrochloric, hydrobromic, sulfuric, sulfamic,
  • Prodrugs of the compounds of the invention may be analogous to the prodrugs of sertindole disclosed in our International Patent Application WO 92/06089, or they may be esters of C 1 - C 18 carboxylic acids formed with possible hydroxy groups on
  • both substituents of at least one pair of substituents are different from hydrogen or constitute together an oxo group.
  • novel compounds of formula I are prepared by a method comprising:
  • the oxo compounds IV and V are conveniently reduced to the corresponding hydroxy compounds using LiAlH 4 , AlH 3 , B 2 H 6 or a BH 3 complex under mild conditions, such as cooling in inert solvents as e.g. diethyl ether or dry tetrahydrofuran. Preparation of the oxo compounds is described in the Examples.
  • Compounds with bifunctional groups VII are e.g. oxalic acid derivatives such as oxalyl chloride or oxalic acid esters or glyoxylic acid derivatives.
  • oxalic acid derivatives such as oxalyl chloride or oxalic acid esters or glyoxylic acid derivatives.
  • the reaction of these derivatives with VI is conveniently performed under acidic or neutral conditions.
  • reaction of a compound of Formula VIII with an alcohol R 1 OH is conveniently performed in an inert solvent, or with the alcohol as solvent at room temperature or at elevated temperature.
  • Protecting groups Z in Formulas IX-XI are removed by methods such as cleavage of a trialkylsilyl protection group with tetraalkylammonium fluoride in an inert solvent or by mild aqueous hydrolysis. Benzyl groups are removed by catalytic hydrogenation using e.g. Pd as a catalyst. Carboxylic acid esters are hydrolyzed under mild neutral or basic conditions well-known to a chemist skilled in the art. The intermediates of Formulas IX-XI may be obtained by methods conventional in the art.
  • Phosgene as the carbonyl precursor is used at low temperatures in inert solvents such as toluene, tetrahydrofuran, diethyl ether optionally in the presence of a base, such as triethylamine or potassium carbonate.
  • inert solvents such as toluene, tetrahydrofuran, diethyl ether optionally in the presence of a base, such as triethylamine or potassium carbonate.
  • the acid addition salts of the compounds of the invention are easily prepared by methods well known in the art.
  • the base is reacted with either the calculated amount of organic or inorganic acid in an aqueous miscible solvent, such as acetone or ethanol, with isolation of the salt by concentration and cooling, or reacted with an excess of the acid in an aqueous immiscible solvent such as ethyl ether or chloroform, with the desired salt separating directly.
  • aqueous miscible solvent such as acetone or ethanol
  • an aqueous immiscible solvent such as ethyl ether or chloroform
  • the compounds of general Formula I , the prodrugs thereof and the pharmaceutically acceptable acid addition salts thereof may be administered in any suitable way, e.g. orally or parenterally, and the compounds may be presented in any suitable form for such administration, e.g. in the form of tablets, capsules, powders, syrups or solutions or dispersions for injection.
  • the prodrugs may conveniently be administered as depot preparations for injection, dissolved in proper oils.
  • An effective daily dose of the a compound of general Formula I or a pharmaceutically acceptable salt thereof is from 10 ⁇ g/kg to 10 mg/kg body weight.
  • the remaining crude product was purified by column chromatography on silica gel using a mixture of ethyl acetate/ethanol/triethylamine (90:10:4) as eluent.
  • the resulting pure hydantoin derivative was recrystallized from ethyl acetate. Yield: 21 g, mp: 165-166 °C.
  • the thus obtained hydantoin derivative (7 g) was dissolved in dry THF (250 ml). A solution of LiAlH 4 (0.7 g) in dry THF (50 ml) was added dropwise at 5-10 °C. The mixture was finally stirred for 5 hours at room temperature.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4 using 5c as starting material. Mp.: 159-62 °C.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4c using 6b as starting material.
  • N-(2-benzyloxyethyl)-2-bromo-2-methylpropionamide as an oil: 104 g
  • a mixture of the crude amide (104 g), sodium azide (23.6 g) and N -methyl-2-pyrrolidone (500 ml) was heated at 50 °C for 22 h. After cooling to room temperatur water was added and the resulting mixture was extracted with diethyl ether (2 X 400 ml). The combined organic phases were washed with brine (3 X 500 ml) and dried (Na 2 SO 4 ).
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4c using 8a as starting material.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4 using 8b as starting material: mp 142-144 °C;
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 9a using 2-[4-[5-chloro-1-(4-fluorophenyl)-1H-indol-3-yl]piperidin-1-yl]ethylamine (prepared as described for similar compounds in J . Med . Chem . 1992 , 35 , 4813-4822) as starting material.
  • the compound was precipitated as its triethylammonium salt from ethyl acetate.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4c using 12b as starting material.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4 using 12c as starting material: mp 176-178 °C;
  • Benzyloxyacetylchloride (16.7 g) was added to a mixture of 1-aminocyclopentan-1-carboxamide (10.2 g), K 2 CO 3 (13.3 g) and acetone (150 ml) at -5 to 0 °C. After stirring at room temperature for 2 h the reaction mixture was filtered. The precipitate was extracted with diethyl ether (50 ml) washed with water (100 ml) and dried at 50 °C in vacuo for 18 h giving the title compound as a crystalline material: 13.8 g.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 12b using 13a as starting material.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4c using 13b as starting material.
  • This compound was prepared by a procedure analogous to the procedure described for the synthesis of 4 using 13c as starting material: mp 143-145 °C;
  • Quipazine is a 5-HT 2 agonist, which induces head twitches in rats.
  • the test is an in vivo test for 5-HT 2 -antagonistic effect measuring the ability to inhibit quipazine induced head twitches.
  • the method and test results for some reference substances are published by Arnt et al. ( Drug Development Research, 16 , 59-70, 1989, attached). The results are shown in Table 2.
  • Some of the compounds of the invention have also been found to inhibit the firing of spontaneously active DA neurones in the ventral tegmental area of the brain upon 21 days of repeated oral treatment of rats.
  • the test wich was performed according to the method described by Skarsfeldt, T. and Perregaard, J., Eur. J. Pharmacol. 1990 , 182, 613-614 is indicative of antipsychotic effects in humans.
  • the pharmaceutical formulations of the invention may be prepared by conventional methods in the art.
  • Tablets may be prepared by mixing the active ingredient with ordinary adjuvants and/or diluents and subsequently compressing the mixture in a conventional tabletting machine.
  • adjuvants or diluents comprise: corn starch, lactose, talcum, magnesium stearate, gelatine, lactose, gums, and the like. Any other adjuvant or additive colourings, aroma, preservatives etc. may be used provided that they are compatible with the active ingredients.
  • Solutions for injections may be prepared by solving the active ingredient and possible additives in a part of the vehicle, preferably sterile water, adjusting the solution to the desired volume, sterilization of the solution and filling in suitable ampules or vials. Any suitable additive conventionally used in the art may be added, such as tonicity agents, preservatives, antioxidants, etc.
  • Typical examples of recipes for the formulations of the invention are as follows: 1) Tablets containing 5 milligrams of Compound 6 calculated as the free base: Compound 6 5.0 mg Lactose 60 mg Maize starch 30 mg Hydroxypropylcellulose 2.4 mg Microcrystalline cellulose 19.2 mg Croscarmellose Sodium Type A 2.4 mg Magnesium stearate 0.84 mg 2) Tablets containing 1 milligram of Compound 8 calculated as the free base: Compound 8 1.0 mg Lactose 46.9 mg Maize starch 23.5 mg Povidone 1.8 mg Microcrystalline cellulose 14.4 mg Croscarmellose Sodium Type A 1.8 mg Magnesium stearate 0.63 mg 3) Syrup containing per millilitre: Compound 4 5.0 mg Sorbitol 500 mg Hydroxypropylcellulose 15 mg Glycerol 50 mg Methyl-paraben 1 mg Propyl-paraben 0.1 mg Ethanol 0.005 ml Flavour 0.05 mg Saccharin natrium 0.5 mg Water

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  • Health & Medical Sciences (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
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  • Psychiatry (AREA)
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  • Polyurethanes Or Polyureas (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Claims (5)

  1. Composé de phénylindole ayant la formule générale I
    Figure 00330001
    où R1 - R4 sont choisis indépendamment dans le groupe consistant en l'hydrogène, le deutérium, alkyle en C1-4 et alcoxy inférieur en C1-4, à condition que les quatre substituants ne puissent pas être tous l'hydrogène; ou
    au moins une paire de substituants (R1, R2 ou R3, R4) constitue un groupe oxo et, si un seul groupe oxo est présent, les deux autres substituants sont choisis dans le groupe défini ci-dessus pour R1 - R4, à condition qu'ils ne puissent pas être tous les deux l'hydrogène; ou
    R1 et R2 et/ou R3 et R4, respectivement, sont liés l'un à l'autre pour former un cycle spiro à 3-8 chaínons;
    ou sel d'addition d'acide de celui-ci.
  2. Composé selon la revendication 1 caractérisé en ce que les deux substituants d'au moins une paire de substituants (R1, R2 ou R3, R4) sont l'un et l'autre différents de l'hydrogène ou constituent ensemble un groupe oxo ou sont liés pour former un cycle spiro.
  3. Composé selon la revendication 1 choisi parmi
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-5-méthoxyimidazolidin-2-one,
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-4,4,5,5-tétradeutéroimidazolidin-2-one,
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-4,4-dideutéroimidazolidin-2-one,
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-5,5-dideutéroimidazolidin-2-one,
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl)-4,4-diméthylimidazolidin-2-one,
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-5,5-diméthylimidazolidin-2-one,
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-5,5-diméthylimidazolidine-2,4-dione,
    la 3-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-1,3-diazaspiro[4.4]nonan-2-one ou
    la 1-[2-[4-[5-chloro-1-(4-fluorophényl)-1H-indol-3-yl]-pipéridin-1-yl]éthyl]-1,3-diazaspiro[4.4]nonan-2-one.
  4. Composition pharmaceutique caractérisée en ce qu'elle comprend un composé selon l'une quelconque des revendications 1 - 3 ainsi qu'un support ou diluant pharmaceutiquement acceptable.
  5. Utilisation d'un composé selon l'une quelconque des revendications 1 - 3 pour préparer une composition pharmaceutique pour le traitement de la psychose, de la dépression, des symptômes négatifs de la schizophrénie, de l'hypertension ou des effets secondaires extrapyramidaux induits par des médicaments neuroleptiques.
EP94931520A 1993-11-01 1994-10-28 Composes de phenylindole Expired - Lifetime EP0726898B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SI9430356T SI0726898T1 (en) 1993-11-01 1994-10-28 Phenylindole compounds

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DK931234A DK123493D0 (da) 1993-11-01 1993-11-01 Compounds
DK1234/93 1993-11-01
DK123493 1993-11-01
PCT/DK1994/000407 WO1995012591A1 (fr) 1993-11-01 1994-10-28 Composes de phenylindole

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EP0726898B1 true EP0726898B1 (fr) 2000-12-20

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US (1) US5703087A (fr)
EP (1) EP0726898B1 (fr)
JP (1) JP3898219B2 (fr)
KR (1) KR100350550B1 (fr)
CN (1) CN1134149A (fr)
AT (1) ATE198199T1 (fr)
AU (1) AU683700B2 (fr)
CA (1) CA2175498C (fr)
CZ (1) CZ291403B6 (fr)
DE (1) DE69426462T2 (fr)
DK (2) DK123493D0 (fr)
ES (1) ES2154303T3 (fr)
FI (1) FI116623B (fr)
GR (1) GR3035462T3 (fr)
HK (1) HK1013817A1 (fr)
HU (1) HUT76063A (fr)
IL (2) IL111395A (fr)
LV (1) LV12805B (fr)
NO (1) NO309038B1 (fr)
NZ (1) NZ275086A (fr)
PL (1) PL176391B1 (fr)
PT (1) PT726898E (fr)
RU (1) RU2156249C2 (fr)
SI (1) SI0726898T1 (fr)
SK (1) SK281761B6 (fr)
WO (1) WO1995012591A1 (fr)
ZA (1) ZA948589B (fr)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011069951A1 (fr) * 2009-12-11 2011-06-16 Glaxo Group Limited Dérivés d'imidazolidinedione
US9422252B2 (en) 2012-05-22 2016-08-23 Autifony Therapeutics Limited Triazoles as Kv3 inhibitors
US9669030B2 (en) 2012-05-22 2017-06-06 Autifony Therapeutics Limited Hydantoin derivatives as Kv3 inhibitors
US10098881B2 (en) 2010-12-06 2018-10-16 Autifony Therapeutics Limited Compounds

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6489341B1 (en) 1999-06-02 2002-12-03 Sepracor Inc. Methods for the treatment of neuroleptic and related disorders using sertindole derivatives
PT1214312E (pt) 1999-09-09 2004-08-31 Lundbeck & Co As H Indoles 5-aminoalquilo e 5-aminocarbonilo substituidos
US20070212412A1 (en) * 2005-09-08 2007-09-13 H. Lundbeck A/S Stable solid formulation of sertindole
TW200821296A (en) * 2006-06-01 2008-05-16 Lundbeck & Co As H Use of sertindole for the preventive treatment of suicidal behaviour
EP2582698B1 (fr) 2010-06-16 2016-09-14 Vitae Pharmaceuticals, Inc. Hétérocycles à 5, 6 et 7 chaînons substitués, médicaments contenant ces composés et leur utilisation
JP6008953B2 (ja) * 2011-06-07 2016-10-19 アウトイフオンイ トヘラペウトイクス リミテッド Ｋｖ３阻害剤としてのヒダントイン誘導体
CN103974944B (zh) * 2011-12-06 2016-11-02 奥蒂福尼疗法有限公司 用作kv3抑制剂的乙内酰脲衍生物

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE58370B1 (en) * 1985-04-10 1993-09-08 Lundbeck & Co As H Indole derivatives
GB8908085D0 (en) * 1989-04-11 1989-05-24 Lundbeck & Co As H New therapeutic use
DK152090D0 (da) * 1990-06-22 1990-06-22 Lundbaek A S H Piperidylsubstituerede indolderivater

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10632118B2 (en) 2009-12-11 2020-04-28 Autifony Therapeutics Limited Imidazolidinedione derivatives
EA019970B1 (ru) * 2009-12-11 2014-07-30 Отифони Терапеутикс Лимитед Производные имидазолидиндиона
EA019970B8 (ru) * 2009-12-11 2014-11-28 Отифони Терапеутикс Лимитед Производные имидазолидиндиона
WO2011069951A1 (fr) * 2009-12-11 2011-06-16 Glaxo Group Limited Dérivés d'imidazolidinedione
US10058551B2 (en) 2009-12-11 2018-08-28 Autifony Therapeutics Limited Imidazolidinedione derivatives
US11583527B2 (en) 2010-12-06 2023-02-21 Autifony Therapeutics Limited Hydantoin derivatives useful as Kv3 inhibitors
US10098881B2 (en) 2010-12-06 2018-10-16 Autifony Therapeutics Limited Compounds
US11197859B2 (en) 2010-12-06 2021-12-14 Autifony Therapeutics Limited Hydantoin derivatives useful as Kv3 inhibitors
US10265316B2 (en) 2010-12-06 2019-04-23 Autifony Therapeuctics Limited Hydantoin derivatives useful as Kv3 inhibitors
US9422252B2 (en) 2012-05-22 2016-08-23 Autifony Therapeutics Limited Triazoles as Kv3 inhibitors
US10611735B2 (en) 2012-05-22 2020-04-07 Autifony Therapeutics Limited Triazoles as Kv3 inhibitors
US11180461B2 (en) 2012-05-22 2021-11-23 Autifony Therapeutics Limited Triazoles as Kv3 inhibitors
US10160730B2 (en) 2012-05-22 2018-12-25 Autifony Therapeutics Limited Triazoles as KV3 inhibitors
US9669030B2 (en) 2012-05-22 2017-06-06 Autifony Therapeutics Limited Hydantoin derivatives as Kv3 inhibitors

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KR960705814A (ko) 1996-11-08
PL314181A1 (en) 1996-08-19
HUT76063A (en) 1997-06-30
JP3898219B2 (ja) 2007-03-28
GR3035462T3 (en) 2001-05-31
NO961746D0 (no) 1996-04-30
NZ275086A (en) 1997-10-24
ATE198199T1 (de) 2001-01-15
CN1134149A (zh) 1996-10-23
CA2175498A1 (fr) 1995-05-11
SK281761B6 (sk) 2001-07-10
PT726898E (pt) 2001-05-31
PL176391B1 (pl) 1999-05-31
LV12805B (lv) 2002-05-20
AU8057794A (en) 1995-05-23
FI961844A (fi) 1996-04-30
KR100350550B1 (ko) 2002-12-12
ZA948589B (en) 1995-06-26
AU683700B2 (en) 1997-11-20
DE69426462T2 (de) 2001-04-26
ES2154303T3 (es) 2001-04-01
DK123493D0 (da) 1993-11-01
US5703087A (en) 1997-12-30
DE69426462D1 (de) 2001-01-25
EP0726898A1 (fr) 1996-08-21
IL111395A0 (en) 1994-12-29
SI0726898T1 (en) 2001-04-30
CZ124896A3 (en) 1996-09-11
NO961746L (no) 1996-06-28
WO1995012591A1 (fr) 1995-05-11
LV12805A (en) 2002-03-20
IL111394A0 (en) 1994-12-29
FI961844A0 (fi) 1996-04-30
HU9601144D0 (en) 1996-07-29
RU2156249C2 (ru) 2000-09-20
HK1013817A1 (en) 1999-09-10
IL111394A (en) 1998-08-16
FI116623B (fi) 2006-01-13
IL111395A (en) 1999-06-20
CZ291403B6 (cs) 2003-03-12
SK53496A3 (en) 1996-11-06
JPH09506083A (ja) 1997-06-17
NO309038B1 (no) 2000-12-04
CA2175498C (fr) 2005-07-26
DK0726898T3 (da) 2001-04-30

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